دورية أكاديمية

Small intestine bleeding due to multifocal angiosarcoma.

التفاصيل البيبلوغرافية
العنوان: Small intestine bleeding due to multifocal angiosarcoma.
المؤلفون: Zacarias Föhrding L; Department of General, Visceral and Pediatric Surgery, Heinrich-Heine-University, Düsseldorf, Moorenstrasse 5, 40225 Düsseldorf, Germany., Macher A, Braunstein S, Knoefel WT, Topp SA
المصدر: World journal of gastroenterology [World J Gastroenterol] 2012 Nov 28; Vol. 18 (44), pp. 6494-500.
نوع المنشور: Case Reports; Journal Article
اللغة: English
بيانات الدورية: Publisher: Baishideng Publishing Group Country of Publication: United States NLM ID: 100883448 Publication Model: Print Cited Medium: Internet ISSN: 2219-2840 (Electronic) Linking ISSN: 10079327 NLM ISO Abbreviation: World J Gastroenterol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2014- : Pleasanton, CA : Baishideng Publishing Group
Original Publication: Beijing : WJG Press, c1998-
مواضيع طبية MeSH: Gastrointestinal Hemorrhage/*etiology , Hemangiosarcoma/*complications , Jejunal Neoplasms/*complications, Aged, 80 and over ; Anemia/etiology ; Biomarkers, Tumor/analysis ; Biopsy ; Blood Transfusion ; Chemotherapy, Adjuvant ; Gastrointestinal Hemorrhage/therapy ; Hemangiosarcoma/chemistry ; Hemangiosarcoma/pathology ; Hemangiosarcoma/surgery ; Hemostatic Techniques ; Humans ; Jejunal Neoplasms/chemistry ; Jejunal Neoplasms/pathology ; Jejunal Neoplasms/surgery ; Jejunostomy ; Male ; Melena/etiology ; Treatment Outcome
مستخلص: We report a case of an 84-year-old male patient with primary small intestinal angiosarcoma. The patient initially presented with anemia and melena. Consecutive endoscopy revealed no signs of upper or lower active gastrointestinal bleeding. The patient had been diagnosed 3 years previously with an aortic dilation, which was treated with a stent. Computed tomography suggested an aorto-intestinal fistula as the cause of the intestinal bleeding, leading to operative stent explantation and aortic replacement. However, an aorto-intestinal fistula was not found, and the intestinal bleeding did not arrest postoperatively. The constant need for blood transfusions made an exploratory laparotomy imperative, which showed multiple bleeding sites, predominately in the jejunal wall. A distal loop jejunostomy was conducted to contain the small intestinal bleeding and a segmental resection for histological evaluation was performed. The histological analysis revealed a less-differentiated tumor with characteristic CD31, cytokeratin, and vimentin expression, which led to the diagnosis of small intestinal angiosarcoma. Consequently, the infiltrated part of the jejunum was successfully resected in a subsequent operation, and adjuvant chemotherapy with paclitaxel was planned. Angiosarcoma of the small intestine is an extremely rare malignant neoplasm that presents with bleeding and high mortality. Early diagnosis and treatment are essential to improve outcome. A small intestinal angiosarcoma is a challenging diagnosis to make because of its rarity, nonspecific symptoms of altered intestinal function, nonspecific abdominal pain, severe melena, and acute abdominal signs. Therefore, a quick clinical and histological diagnosis and decisive measures including surgery and adjuvant chemotherapy should be the aim.
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فهرسة مساهمة: Keywords: Angiosarcoma; Gastrointestinal bleeding; Small intestinal neoplasm; Small intestine
المشرفين على المادة: 0 (Biomarkers, Tumor)
تواريخ الأحداث: Date Created: 20121201 Date Completed: 20131114 Latest Revision: 20211021
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC3508646
DOI: 10.3748/wjg.v18.i44.6494
PMID: 23197897
قاعدة البيانات: MEDLINE
الوصف
تدمد:2219-2840
DOI:10.3748/wjg.v18.i44.6494